Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

Feifei Tao(University of Miami), Stephan Züchner(University of Miami), Gary W. Beecham(University of Miami), Mary M. Reilly(University College London), Sabrina W. Yum(Children's Hospital of Philadelphia), Camila Lopez‐Anido(University of Wisconsin–Madison), John Svaren(University of Wisconsin–Madison), Michael E. Shy(University of Iowa), Mario Saporta(University of Miami), Susan H. Blanton(University of Miami), Devon Rizzo(University of South Florida), Frank Baas(The Netherlands Cancer Institute), Thomas E. Lloyd(Johns Hopkins University), Byung‐Ok Choi(Yonsei University), Davide Pareyson(Unknown), Adriana Rebelo(University of Miami), Jasper M. Morrow(National Hospital for Neurology and Neurosurgery), Shawna Feely(Wayne State University), Camiel Verhamme(Unknown), John J. Moran(University of Wisconsin–Madison), Franco Taroni(Fondazione IRCCS Istituto Neurologico Carlo Besta), Jun Li(Wayne State University), David N. Herrmann(University of Rochester Medical Center), Lisa Abreu(University of Miami), Charlotte J. Sumner(Johns Hopkins University), Callyn A. Kirk(University of South Florida), Xingyao Wu(University of Iowa), Steven S. Scherer(University of Pennsylvania)
Annals of Neurology
February 1, 2019
Cited by 45


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